CN1138486A - Method for prodn. of medical dyeing dressing - Google Patents
Method for prodn. of medical dyeing dressing Download PDFInfo
- Publication number
- CN1138486A CN1138486A CN 96102345 CN96102345A CN1138486A CN 1138486 A CN1138486 A CN 1138486A CN 96102345 CN96102345 CN 96102345 CN 96102345 A CN96102345 A CN 96102345A CN 1138486 A CN1138486 A CN 1138486A
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- China
- Prior art keywords
- aqueous solution
- grams per
- per liter
- solution
- liter aqueous
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000004043 dyeing Methods 0.000 title claims abstract description 11
- 238000000034 method Methods 0.000 title claims description 14
- 239000002250 absorbent Substances 0.000 claims abstract description 13
- 230000002745 absorbent Effects 0.000 claims abstract description 13
- 231100000252 nontoxic Toxicity 0.000 claims abstract description 4
- 230000003000 nontoxic effect Effects 0.000 claims abstract description 4
- 239000007864 aqueous solution Substances 0.000 claims description 45
- 239000000243 solution Substances 0.000 claims description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 21
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 claims description 18
- 239000000975 dye Substances 0.000 claims description 16
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 claims description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 12
- 238000006386 neutralization reaction Methods 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 7
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- 238000005406 washing Methods 0.000 claims description 7
- 229960000583 acetic acid Drugs 0.000 claims description 6
- 239000012362 glacial acetic acid Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 claims description 6
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 claims description 6
- 238000009835 boiling Methods 0.000 claims description 5
- 239000000344 soap Substances 0.000 claims description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 235000019239 indanthrene blue RS Nutrition 0.000 claims description 3
- LIBWRRJGKWQFSD-UHFFFAOYSA-M sodium;2-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=CC=C1S([O-])(=O)=O LIBWRRJGKWQFSD-UHFFFAOYSA-M 0.000 claims description 3
- UGCDBQWJXSAYIL-UHFFFAOYSA-N vat blue 6 Chemical compound O=C1C2=CC=CC=C2C(=O)C(C=C2Cl)=C1C1=C2NC2=C(C(=O)C=3C(=CC=CC=3)C3=O)C3=CC(Cl)=C2N1 UGCDBQWJXSAYIL-UHFFFAOYSA-N 0.000 claims description 2
- 239000008280 blood Substances 0.000 abstract description 4
- 210000004369 blood Anatomy 0.000 abstract description 4
- 238000011084 recovery Methods 0.000 description 3
- OOXHZCGBJSGVTN-UHFFFAOYSA-N 4,5,6-trichloro-3h-1,3-benzoxazol-2-one Chemical compound ClC1=C(Cl)C(Cl)=CC2=C1NC(=O)O2 OOXHZCGBJSGVTN-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000009970 yarn dyeing Methods 0.000 description 2
- 230000003187 abdominal effect Effects 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
Landscapes
- Coloring (AREA)
Abstract
A coloured medical dressing is made up by dyeing white absorbent gauze into green or blue with non-toxic dye. The blood adsorbed by said colour gauze shows black or dark colour, eliminating the fear of patient. As its colour is obviously different from that of human organa, it is easy to recover the used dressing after operating.
Description
The present invention relates to the manufacture method of dyed medical dressing material.
Medical dressing of the prior art generally adopts white absorbent carbasus.This dressing in use, because of catching the fear that BRB easily causes patient.In addition, stained in abdominal operation with blood red dressing is difficult to discern and the recovery of checking that is unfavorable for the medical worker.
The objective of the invention is at the problems referred to above provide a kind of can reduce patient's fear and be convenient to perform the operation in medical worker's manufacture method of checking the dyed medical dressing material of recovery.
Technical scheme of the present invention is that a kind of manufacture method of dyed medical dressing material, its main points are to adopt non-toxic dye that white absorbent carbasus is dyed green or blue medical dressing.
And above-mentioned process of dying absorbent carbasus comprises: dyeing, oxidation, washing, soap boiling, neutralization, oven dry.
And, above-mentioned dyeing is that absorbent carbasus is being comprised Deco that SN-S (DEKOL SN-S) 1.2～2.5 grams per liter aqueous solutions, Te Lielan TB (TRILAN TB) 0.5～1.5 grams per liter aqueous solution, Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS) 0.5～1.5 grams per liter aqueous solution, Peregal P (PEREGAL P) 0.5～1.5 grams per liter aqueous solution, sodium hydrosulfite (85%) 0.5～5 grams per liter aqueous solution, dyed at normal temperatures 15～20 minutes with 0.7～2.8% (percentage by weight of dyestuff and gauze) indanthrene blue CLF or indanthrene blue BC (INDANTHRENE BLUE CLF or BC) in the solution of 5～25 milliliters/premium on currency solution of sodium hydroxide (36 ° of Be '), dyed 30～55 minutes at 45～60 ℃ then.
And, sodium hydroxide in the above-mentioned solution (36 ° of Be ') is 15～25 milliliters/premium on currency solution, sodium hydrosulfite (85%) 1.2～2.2 grams per liter aqueous solution, and used indanthrene blue CLF or BC (INDAN-THRENE BLUE CLF or BC) are 1.2～2.8% (percentage by weights of dyestuff and gauze).
Perhaps, 5～10 milliliters/premium on currency solution of sodium hydroxide in the solution (36 ° of Be '), indanthrene blue CLF or BC (INDANTHRENE BLUE CLF or BC) are 0.7～2.0% (percentage by weight of dyestuff and gauze, down together), simultaneously, also add dyestuff flavanthrone 5GF (INDAN-THRENE YELLOW 5GF) 0.3～1.3%.
And, above-mentioned dyed gauze is being contained Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS) 0.5～1.5 grams per liter aqueous solution, land Di Geer (LUDIGOL) 1.5～3.5 grams per liter aqueous solutions, 27% hydrogen peroxide (H
2O
2) carrying out oxidation in 1.5～2.3 milliliters/premium on currency solution, the aqueous solution of 0.2～0.8 milliliter/premium on currency of 30% glacial acetic acid solution, reaction condition is: 45～60 ℃ of temperature, 10～30 minutes time, PH=9; Then at normal temperatures with the aqueous solution washing that contains 0.5～1.5 grams per liter aqueous solution Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS), you SN-S (DEKOL SN-S) of 0.5～1.5 grams per liter aqueous solution Deco 10 minutes; Boiled 10～30 minutes with the aqueous solution that contains 0.5～1.5 grams per liter aqueous solution Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS), you SN-S (DEKOL SN-S) of 1.2～2.5 grams per liter aqueous solution Decos down at 80～100 ℃; Reuse glacial acetic acid neutralization make PH be 6.5～7.2 backs 80～150 ℃ of oven dry down, put in order at last the dyed medical dressing material finished product.
The present invention is owing to dye green or blue medical dressing with white absorbent carbasus, and like this, during use, the blood that adsorbs on the dyeing gauze will become black or dim dark color.Thereby eliminate the fear of patient to red blood.In addition, owing to dyed medical dressing material color and above-mentioned use variable color and human tissue organ obvious different be convenient to perform the operation in the medical worker check recovery.
Below the present invention is described in further detail.
The present invention adopts non-toxic dye that white absorbent carbasus is dyed green or blue medical dressing.The process of dying absorbent carbasus comprises: dyeing, oxidation, washing, soap boiling, neutralization, oven dry, arrangement.
The present invention's dyeing is that absorbent carbasus is being contained Deco that SN-S (DEKOL SN-S) 1.2～2.5 grams per liter aqueous solutions, Te Lielan TB (TRILAN TB) 0.5～1.5 grams per liter aqueous solution, Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS) 0.5～1.5 grams per liter aqueous solution, Peregal P (PEREGAL P) 0.5～1.5 grams per liter aqueous solution, 85% sodium hydrosulfite, 0.5～5 grams per liter aqueous solution, dye with blueness or green colouring material as required in the solution of 5～25 milliliters/premium on currency of NaOH36 ° of Be ' solution, dyeing condition is: dyed under the room temperature 15～20 minutes, dyed 30～55 minutes at 45～60 ℃ then, the ratio of absorbent carbasus and dye liquor is 1: 15 (percentage by weight).
When making blue dressing, dyestuff can be selected indanthrene blue CLF or BC (INDANTHRENE BLUE CLF or BC) for use, content is preferably 1.2～2.3% (percentage by weights) of institute's yarn dyeing cloth amount, and 6 ° of Be ' of the NaOH3 in the solution are preferably 15～25 milliliters/premium on currency solution, 85% sodium hydrosulfite is preferably 1.2～2.2 grams per liter aqueous solutions.
When making green dressing, dyestuff can be selected indanthrene blue CLF or BC (INEDANTHRENEBLUE CLF or BC) and flavanthrone 5GF (INDANTHRENE YELLOW5GF) for use, its consumption is respectively 0.7～2.0% and 0.3～1.3% (percentage by weight) of institute's yarn dyeing cloth amount, and the NaOH in the solution (36 ° of Be ') is preferably 5～10 milliliters/premium on currency solution.
Above-mentioned dyed gauze is being contained Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS) 0.5～1.5 grams per liter aqueous solution, land Di Geer (LUDIGOL) 1.5～3.5 grams per liter aqueous solutions, 27% hydrogen peroxide
(H
2O
2) carrying out oxidation in 1.5～2.3 milliliters/premium on currency solution, the aqueous solution of 0.2～0.8 milliliter/premium on currency of 30% glacial acetic acid solution, reaction condition is: 45～60 ℃ of temperature, 10～30 minutes time, PH=9; Then at normal temperatures with the aqueous solution washing that contains 0.5～1.5 grams per liter aqueous solution Zero Energy Thermonuclear Assembly (Zeta) Mo Er (SETAMOL WS), you SN-S (DEKOL SN-S) of 0.5～1.5 grams per liter aqueous solution Deco 10 minutes; At 80～100 ℃ down with the aqueous solution soap boiling that contains 0.5～1.5 grams per liter aqueous solution Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS), you SN-S (DEKOLSN-S) of 1.2～2.5 grams per liter aqueous solution Decos 10～30 minutes; Reuse glacial acetic acid neutralization makes PH=6.5～7.2 backs 80～150 ℃ of oven dry down, put in order at last the dyed medical dressing material finished product.
The present invention can choose one group of particular value arbitrarily and make dyed medical dressing material in the above-mentioned parameter scope.Last tabular has gone out several class values as specific embodiment, wherein three class values in the dyeing can with each three class value combination in any of oxidation, washing, soap boiling, neutralization, oven dry, arbitrary class value of getting after the combination can obtain the dyed medical dressing material finished product as stated above.
Claims (6)
1, a kind of manufacture method of dyed medical dressing material is characterized in that adopting non-toxic dye that white absorbent carbasus is dyed green or blue medical dressing.
2, manufacture method according to claim 1 is characterized in that the process of dying absorbent carbasus comprises: dyeing, oxidation, washing, soap boiling, neutralization, oven dry.
3, method according to claim 2, it is characterized in that dyeing is that absorbent carbasus is being comprised Deco that SN-S (DEKOL SN-S) 1.2～2.5 grams per liter aqueous solutions, Te Lielan TB (TRILANTB) 0.5～1.5 grams per liter aqueous solution, Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS) 0.5～1.5 grams per liter aqueous solution, Peregal P (PEREGAL P) 0.5～1.5 grams per liter aqueous solution, sodium hydrosulfite (85%) 0.5～5 grams per liter aqueous solution, indanthrene blue CLF or indanthrene blue BC (INDANTHRENE BLUE CLF or BC) with 0.7～2.8% (percentage by weight of dyestuff and gauze) in the solution of 5～25 milliliters/premium on currency solution of sodium hydroxide (36 ° of Be ') dyed 15～20 minutes at normal temperatures, dyed 30～55 minutes at 45～60 ℃ then.
4, method according to claim 3, it is characterized in that, 36 ° of Be ' of sodium hydroxide in the solution) be 15～25 milliliters/premium on currency solution, sodium hydrosulfite (85%) 1.2～2.2 grams per liter aqueous solution, used indanthrene blue CLF or BC (INDANTHRENE BLUE CLF or BC) are 1.2～2.8% (percentage by weights of dyestuff and gauze).
6, method according to claim 4, it is characterized in that, sodium hydroxide in the solution (36 ° of Be ') is 5～10 a milliliters/premium on currency solution, indanthrene blue CLF or BC (INDANTHRENEBLUE CLF or BC) are 0.7～2.0% (percentage by weight of dyestuff and gauze, also add dyestuff flavanthrone 5GF (INDANTHRENE YELLOW 5GF) 0.3～1.3% simultaneously down together).
7, according to the described arbitrary method of claim 1～6, it is characterized in that, above-mentioned dyed gauze is being contained Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS) 0.5～1.5 grams per liter aqueous solution, land Di Geer (LUDIGOL) 1.5～3.5 grams per liter aqueous solutions, 27% hydrogen peroxide (H
2O
2) carrying out oxidation in 1.5～2.3 milliliters/premium on currency solution, the aqueous solution of 0.2～0.8 milliliter/premium on currency of 30% glacial acetic acid solution, reaction condition is: 45～60 ℃ of temperature, 10～30 minutes time, PH=9; Then at normal temperatures with the aqueous solution washing that contains 0.5～1.5 grams per liter aqueous solution Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS), you SN-S (DEKOL SN-S) of 0.5～1.5 grams per liter aqueous solution Deco 10 minutes; Boiled 10～30 minutes with the aqueous solution that contains 0.5～1.5 grams per liter aqueous solution Zero Energy Thermonuclear Assembly (Zeta) Mo Er WS (SETAMOL WS), you SN-S (DEKOL SN-S) of 1.2～2.5 grams per liter aqueous solution Decos down at 80～100 ℃; Reuse glacial acetic acid neutralization make PH be 6,5～7.2 backs 80～150 ℃ of oven dry down, put in order at last the dyed medical dressing material finished product.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN96102345A CN1067278C (en) | 1996-07-12 | 1996-07-12 | Method for prodn. of medical dyeing dressing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN96102345A CN1067278C (en) | 1996-07-12 | 1996-07-12 | Method for prodn. of medical dyeing dressing |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1138486A true CN1138486A (en) | 1996-12-25 |
| CN1067278C CN1067278C (en) | 2001-06-20 |
Family
ID=5117503
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN96102345A Expired - Fee Related CN1067278C (en) | 1996-07-12 | 1996-07-12 | Method for prodn. of medical dyeing dressing |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1067278C (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101193613B (en) * | 2005-06-08 | 2011-04-27 | 卡尔·奥托·布劳恩两合公司 | Dressing material and method for its production |
| WO2011049522A1 (en) * | 2009-10-20 | 2011-04-28 | Mölnlycke Health Care Ab | Green article for use in wound treatment |
| CN101612417B (en) * | 2009-07-14 | 2012-11-14 | 湖北琪美医疗科技有限公司 | Production method of dyed medical dressing material |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0375810A1 (en) * | 1988-12-29 | 1990-07-04 | Cornelia Gesina Maria Fischer-Schreiner | Adhesive plaster and bandage for medical purposes, as well as methods of manufacturing them |
-
1996
- 1996-07-12 CN CN96102345A patent/CN1067278C/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101193613B (en) * | 2005-06-08 | 2011-04-27 | 卡尔·奥托·布劳恩两合公司 | Dressing material and method for its production |
| CN101612417B (en) * | 2009-07-14 | 2012-11-14 | 湖北琪美医疗科技有限公司 | Production method of dyed medical dressing material |
| WO2011049522A1 (en) * | 2009-10-20 | 2011-04-28 | Mölnlycke Health Care Ab | Green article for use in wound treatment |
| US20120203145A1 (en) * | 2009-10-20 | 2012-08-09 | Molnlycke Health Care Ab | Green article for use in wound treatment |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1067278C (en) | 2001-06-20 |
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| C53 | Correction of patent for invention or patent application | ||
| CB02 | Change of applicant information |
Applicant after: Xiantao City Sanitary Material Factory, Hubei Applicant before: Li Xiaoquan Applicant before: Peng Xiyun |
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Free format text: CORRECT: APPLICANT; FROM: LI XIAOQUAN PENG XIYUN TO: XIANTAO CITY SANITARY MATERIAL FACTORY, HUBEI |
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| C14 | Grant of patent or utility model | ||
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Free format text: CORRECT: PATENTEE; FROM: XIANTAO CITY SANITARY MATERIAL FACTORY, HUBEI TO: HUBEI QIMEI TREATMENT SCIENCE CO., LTD. |
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| CP01 | Change in the name or title of a patent holder |
Patentee after: Hubei Qimei Medical Science and Technology Co., Ltd. Patentee before: Xiantao City Sanitary Material Factory, Hubei |
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| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20010620 Termination date: 20130712 |